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You searched for subject:(Transcription factor NF Y). Showing records 1 – 30 of 79037 total matches.

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Harvard University

1. Fleming, Joseph. Genome-wide Integrative Analysis of Transcription Factor Occupancy and Gene Regulation in Models of Human Cancer and Cellular Differentiation.

Degree: PhD, Biological Sciences in Dental Medicine, 2012, Harvard University

 Few transcription factors (TFs) have been studied in the context of an integrative analysis incorporating genomic datasets from diverse genome regulatory mechanisms. Such an analysis… (more)

Subjects/Keywords: ChIP; FOS; NF-Y; STAT3; molecular biology; bioinformatics; biology; cancer; transcription

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Fleming, J. (2012). Genome-wide Integrative Analysis of Transcription Factor Occupancy and Gene Regulation in Models of Human Cancer and Cellular Differentiation. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:9920185

Chicago Manual of Style (16th Edition):

Fleming, Joseph. “Genome-wide Integrative Analysis of Transcription Factor Occupancy and Gene Regulation in Models of Human Cancer and Cellular Differentiation.” 2012. Doctoral Dissertation, Harvard University. Accessed July 17, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:9920185.

MLA Handbook (7th Edition):

Fleming, Joseph. “Genome-wide Integrative Analysis of Transcription Factor Occupancy and Gene Regulation in Models of Human Cancer and Cellular Differentiation.” 2012. Web. 17 Jul 2019.

Vancouver:

Fleming J. Genome-wide Integrative Analysis of Transcription Factor Occupancy and Gene Regulation in Models of Human Cancer and Cellular Differentiation. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2019 Jul 17]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9920185.

Council of Science Editors:

Fleming J. Genome-wide Integrative Analysis of Transcription Factor Occupancy and Gene Regulation in Models of Human Cancer and Cellular Differentiation. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9920185

2. 椎村, 祐樹. Regulation of the Human Ghrelin Promoter Activity by Transcription Factors, NF-κB and Nkx2.2 : グレリンのプロモーター活性は、NF-κB および Nkx2.2によって制御される.

Degree: 博士(医学), 2018, Kurume University / 久留米大学

2014年度

Subjects/Keywords: ghrelin; transcription factor; NF-κB; Nkx2.2

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APA (6th Edition):

椎村, . (2018). Regulation of the Human Ghrelin Promoter Activity by Transcription Factors, NF-κB and Nkx2.2 : グレリンのプロモーター活性は、NF-κB および Nkx2.2によって制御される. (Thesis). Kurume University / 久留米大学. Retrieved from http://hdl.handle.net/11316/462

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

椎村, 祐樹. “Regulation of the Human Ghrelin Promoter Activity by Transcription Factors, NF-κB and Nkx2.2 : グレリンのプロモーター活性は、NF-κB および Nkx2.2によって制御される.” 2018. Thesis, Kurume University / 久留米大学. Accessed July 17, 2019. http://hdl.handle.net/11316/462.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

椎村, 祐樹. “Regulation of the Human Ghrelin Promoter Activity by Transcription Factors, NF-κB and Nkx2.2 : グレリンのプロモーター活性は、NF-κB および Nkx2.2によって制御される.” 2018. Web. 17 Jul 2019.

Vancouver:

椎村 . Regulation of the Human Ghrelin Promoter Activity by Transcription Factors, NF-κB and Nkx2.2 : グレリンのプロモーター活性は、NF-κB および Nkx2.2によって制御される. [Internet] [Thesis]. Kurume University / 久留米大学; 2018. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/11316/462.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

椎村 . Regulation of the Human Ghrelin Promoter Activity by Transcription Factors, NF-κB and Nkx2.2 : グレリンのプロモーター活性は、NF-κB および Nkx2.2によって制御される. [Thesis]. Kurume University / 久留米大学; 2018. Available from: http://hdl.handle.net/11316/462

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

3. Patel, Nisha. NF-kappaB in Neuroinflammation.

Degree: 2015, University of Manchester

 The NF-κB stress signalling system has an important role in the control of inflammation, being both stimulated by cytokines and itself regulating cytokine gene expression.… (more)

Subjects/Keywords: neuroinflammation; neural progenitor cells; microglia; NF-kappaB; single-cell; dynamics; transcription factor

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APA (6th Edition):

Patel, N. (2015). NF-kappaB in Neuroinflammation. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259717

Chicago Manual of Style (16th Edition):

Patel, Nisha. “NF-kappaB in Neuroinflammation.” 2015. Doctoral Dissertation, University of Manchester. Accessed July 17, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259717.

MLA Handbook (7th Edition):

Patel, Nisha. “NF-kappaB in Neuroinflammation.” 2015. Web. 17 Jul 2019.

Vancouver:

Patel N. NF-kappaB in Neuroinflammation. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Jul 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259717.

Council of Science Editors:

Patel N. NF-kappaB in Neuroinflammation. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:259717


University of Manchester

4. Patel, Nisha. NF-kappaB in neuroinflammation.

Degree: PhD, 2015, University of Manchester

 The NF-kappaB stress signalling system has an important role in the control of inflammation, being both stimulated by cytokines and itself regulating cytokine gene expression.… (more)

Subjects/Keywords: neuroinflammation; neural progenitor cells; microglia; NF-kappaB; single-cell; dynamics; transcription factor

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APA (6th Edition):

Patel, N. (2015). NF-kappaB in neuroinflammation. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/nfkappab-in-neuroinflammation(2f3b87da-c5e4-4a53-8104-7e5d8162e372).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771317

Chicago Manual of Style (16th Edition):

Patel, Nisha. “NF-kappaB in neuroinflammation.” 2015. Doctoral Dissertation, University of Manchester. Accessed July 17, 2019. https://www.research.manchester.ac.uk/portal/en/theses/nfkappab-in-neuroinflammation(2f3b87da-c5e4-4a53-8104-7e5d8162e372).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771317.

MLA Handbook (7th Edition):

Patel, Nisha. “NF-kappaB in neuroinflammation.” 2015. Web. 17 Jul 2019.

Vancouver:

Patel N. NF-kappaB in neuroinflammation. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Jul 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/nfkappab-in-neuroinflammation(2f3b87da-c5e4-4a53-8104-7e5d8162e372).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771317.

Council of Science Editors:

Patel N. NF-kappaB in neuroinflammation. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/nfkappab-in-neuroinflammation(2f3b87da-c5e4-4a53-8104-7e5d8162e372).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771317

5. Βασιλάκη, Ελευθερία. Μελέτη του μηχανισμού μεταγραφικής ρύθμισης του γονιδίου της μικρής GTPασης RHOB από το μονοπάτι του μετασχηματίζοντα αυξητικού παράγοντα β (TGFβ-1) και ο ρόλος της στις TGFβ-1- επαγώμενες αποκρίσεις του κυττάρου.

Degree: 2009, University of Crete (UOC); Πανεπιστήμιο Κρήτης

Rho proteins are characterized as molecular switches that control many cellular processes including actin and microtubule cytoskeleton organization, cell division, motility, cell adhesion, vesicular trafficking,… (more)

Subjects/Keywords: Μετασχηματίζων αυξητικός παράγοντας β; Μεταγραφική ρύθμιση; Πρωτείνες Smad; Πρωτεΐνες ERK 1/2; Μεταγραφικός παράγοντας NF-Y; Κυτταρική μετακίνηση; Επιθήλιο-μεσεγχυματική μετατροπή των κυττάρων; Κυτταρική ανάπτυξη; RHOB GTPαση; Transforming Growth Factor β; RHOB GTPase; Transcriptional regulation; Smad proteins; ERK1/2 proteins; Transcription factor NF-Y; Cell migration; Epithelial to mesenchymal transition; Cell growth

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APA (6th Edition):

Βασιλάκη, . . (2009). Μελέτη του μηχανισμού μεταγραφικής ρύθμισης του γονιδίου της μικρής GTPασης RHOB από το μονοπάτι του μετασχηματίζοντα αυξητικού παράγοντα β (TGFβ-1) και ο ρόλος της στις TGFβ-1- επαγώμενες αποκρίσεις του κυττάρου. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/18295

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Βασιλάκη, Ελευθερία. “Μελέτη του μηχανισμού μεταγραφικής ρύθμισης του γονιδίου της μικρής GTPασης RHOB από το μονοπάτι του μετασχηματίζοντα αυξητικού παράγοντα β (TGFβ-1) και ο ρόλος της στις TGFβ-1- επαγώμενες αποκρίσεις του κυττάρου.” 2009. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed July 17, 2019. http://hdl.handle.net/10442/hedi/18295.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Βασιλάκη, Ελευθερία. “Μελέτη του μηχανισμού μεταγραφικής ρύθμισης του γονιδίου της μικρής GTPασης RHOB από το μονοπάτι του μετασχηματίζοντα αυξητικού παράγοντα β (TGFβ-1) και ο ρόλος της στις TGFβ-1- επαγώμενες αποκρίσεις του κυττάρου.” 2009. Web. 17 Jul 2019.

Vancouver:

Βασιλάκη . Μελέτη του μηχανισμού μεταγραφικής ρύθμισης του γονιδίου της μικρής GTPασης RHOB από το μονοπάτι του μετασχηματίζοντα αυξητικού παράγοντα β (TGFβ-1) και ο ρόλος της στις TGFβ-1- επαγώμενες αποκρίσεις του κυττάρου. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2009. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10442/hedi/18295.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Βασιλάκη . Μελέτη του μηχανισμού μεταγραφικής ρύθμισης του γονιδίου της μικρής GTPασης RHOB από το μονοπάτι του μετασχηματίζοντα αυξητικού παράγοντα β (TGFβ-1) και ο ρόλος της στις TGFβ-1- επαγώμενες αποκρίσεις του κυττάρου. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2009. Available from: http://hdl.handle.net/10442/hedi/18295

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

6. Thibault, Thomas. Stratégie du leurre moléculaire en thérapie génique : ciblage de facteurs de transcription par un minicercle d'ADN multisites et étude de l'interaction entre l'ADN platiné et NF-κB : Decoy strategy in gene therapy : targeting transcription factors by multisite DNA minicircle and study of the interaction between platinated DNA and NF-κB.

Degree: Docteur es, Biologie, 2012, Université d'Orléans

En thérapie génique, la stratégie du leurre moléculaire consiste à utiliser un acide nucléique courtcontenant une séquence spécifiquement reconnue par un facteur de transcription cible,… (more)

Subjects/Keywords: Leurre moléculaire; Minicercle d’ADN; Thérapie génique; Multiciblage; Facteur de transcription NF-κB; Cisplatine; Decoy; DNA minicircle; Gene therapy; Transcription factor NF-κB; Cisplatin

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APA (6th Edition):

Thibault, T. (2012). Stratégie du leurre moléculaire en thérapie génique : ciblage de facteurs de transcription par un minicercle d'ADN multisites et étude de l'interaction entre l'ADN platiné et NF-κB : Decoy strategy in gene therapy : targeting transcription factors by multisite DNA minicircle and study of the interaction between platinated DNA and NF-κB. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2012ORLE2069

Chicago Manual of Style (16th Edition):

Thibault, Thomas. “Stratégie du leurre moléculaire en thérapie génique : ciblage de facteurs de transcription par un minicercle d'ADN multisites et étude de l'interaction entre l'ADN platiné et NF-κB : Decoy strategy in gene therapy : targeting transcription factors by multisite DNA minicircle and study of the interaction between platinated DNA and NF-κB.” 2012. Doctoral Dissertation, Université d'Orléans. Accessed July 17, 2019. http://www.theses.fr/2012ORLE2069.

MLA Handbook (7th Edition):

Thibault, Thomas. “Stratégie du leurre moléculaire en thérapie génique : ciblage de facteurs de transcription par un minicercle d'ADN multisites et étude de l'interaction entre l'ADN platiné et NF-κB : Decoy strategy in gene therapy : targeting transcription factors by multisite DNA minicircle and study of the interaction between platinated DNA and NF-κB.” 2012. Web. 17 Jul 2019.

Vancouver:

Thibault T. Stratégie du leurre moléculaire en thérapie génique : ciblage de facteurs de transcription par un minicercle d'ADN multisites et étude de l'interaction entre l'ADN platiné et NF-κB : Decoy strategy in gene therapy : targeting transcription factors by multisite DNA minicircle and study of the interaction between platinated DNA and NF-κB. [Internet] [Doctoral dissertation]. Université d'Orléans; 2012. [cited 2019 Jul 17]. Available from: http://www.theses.fr/2012ORLE2069.

Council of Science Editors:

Thibault T. Stratégie du leurre moléculaire en thérapie génique : ciblage de facteurs de transcription par un minicercle d'ADN multisites et étude de l'interaction entre l'ADN platiné et NF-κB : Decoy strategy in gene therapy : targeting transcription factors by multisite DNA minicircle and study of the interaction between platinated DNA and NF-κB. [Doctoral Dissertation]. Université d'Orléans; 2012. Available from: http://www.theses.fr/2012ORLE2069


East Tennessee State University

7. Ngeny, Beverly C. Effects of Lactobacillus rhamnosus Milk Isolate on the Production of Inflammatory Cytokines in Enterocytes.

Degree: MS, Biology, 2016, East Tennessee State University

  In the gastrointestinal tract, probiotics have been shown to promote host immunity and to regulate immune signaling pathways. This study used Caco-2 cell line… (more)

Subjects/Keywords: Caco-2 cells; Inflammatory cytokines; Lactobacillus rhamnosus; NF-kB transcription factor; Probiotics; Bacteriology; Life Sciences; Microbiology; Other Microbiology

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APA (6th Edition):

Ngeny, B. C. (2016). Effects of Lactobacillus rhamnosus Milk Isolate on the Production of Inflammatory Cytokines in Enterocytes. (Masters Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/3027

Chicago Manual of Style (16th Edition):

Ngeny, Beverly C. “Effects of Lactobacillus rhamnosus Milk Isolate on the Production of Inflammatory Cytokines in Enterocytes.” 2016. Masters Thesis, East Tennessee State University. Accessed July 17, 2019. https://dc.etsu.edu/etd/3027.

MLA Handbook (7th Edition):

Ngeny, Beverly C. “Effects of Lactobacillus rhamnosus Milk Isolate on the Production of Inflammatory Cytokines in Enterocytes.” 2016. Web. 17 Jul 2019.

Vancouver:

Ngeny BC. Effects of Lactobacillus rhamnosus Milk Isolate on the Production of Inflammatory Cytokines in Enterocytes. [Internet] [Masters thesis]. East Tennessee State University; 2016. [cited 2019 Jul 17]. Available from: https://dc.etsu.edu/etd/3027.

Council of Science Editors:

Ngeny BC. Effects of Lactobacillus rhamnosus Milk Isolate on the Production of Inflammatory Cytokines in Enterocytes. [Masters Thesis]. East Tennessee State University; 2016. Available from: https://dc.etsu.edu/etd/3027


Montana Tech

8. Mintz, Kathryn Louise. Differences of DNA-Transcription Factor Interactions Following Chromium Exposure.

Degree: MS, 2006, Montana Tech

 The effect of 8-oxoguanine in the consensus sequence of êB DNA on the binding affinity of p50BD was determined using a 22-mer and a 30-mer… (more)

Subjects/Keywords: Chromium; DNA Damage; NF-kB; Transcription Factor Protein

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APA (6th Edition):

Mintz, K. L. (2006). Differences of DNA-Transcription Factor Interactions Following Chromium Exposure. (Masters Thesis). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/319

Chicago Manual of Style (16th Edition):

Mintz, Kathryn Louise. “Differences of DNA-Transcription Factor Interactions Following Chromium Exposure.” 2006. Masters Thesis, Montana Tech. Accessed July 17, 2019. https://scholarworks.umt.edu/etd/319.

MLA Handbook (7th Edition):

Mintz, Kathryn Louise. “Differences of DNA-Transcription Factor Interactions Following Chromium Exposure.” 2006. Web. 17 Jul 2019.

Vancouver:

Mintz KL. Differences of DNA-Transcription Factor Interactions Following Chromium Exposure. [Internet] [Masters thesis]. Montana Tech; 2006. [cited 2019 Jul 17]. Available from: https://scholarworks.umt.edu/etd/319.

Council of Science Editors:

Mintz KL. Differences of DNA-Transcription Factor Interactions Following Chromium Exposure. [Masters Thesis]. Montana Tech; 2006. Available from: https://scholarworks.umt.edu/etd/319


University of Texas – Austin

9. -1768-1645. Novel regulatory mechanisms of nuclear factor (NF)-𝛋B signaling: Novel regulatory mechanisms of nuclear factor (NF)-[kappa] B signaling.

Degree: Cellular and Molecular Biology, 2015, University of Texas – Austin

 Nuclear factor (NF)-𝛋B modulates the transcription of various target genes that are involved in innate and adaptive immune responses, and cell survival. The activation of… (more)

Subjects/Keywords: NF-𝛋B; Nuclear factor signaling; Regulatory mechanisms; Gene transcription; Aberrant activation; Therapeutic interventions; Canonical signaling; Noncanonical signaling

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APA (6th Edition):

-1768-1645. (2015). Novel regulatory mechanisms of nuclear factor (NF)-𝛋B signaling: Novel regulatory mechanisms of nuclear factor (NF)-[kappa] B signaling. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47203

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-1768-1645. “Novel regulatory mechanisms of nuclear factor (NF)-𝛋B signaling: Novel regulatory mechanisms of nuclear factor (NF)-[kappa] B signaling.” 2015. Thesis, University of Texas – Austin. Accessed July 17, 2019. http://hdl.handle.net/2152/47203.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-1768-1645. “Novel regulatory mechanisms of nuclear factor (NF)-𝛋B signaling: Novel regulatory mechanisms of nuclear factor (NF)-[kappa] B signaling.” 2015. Web. 17 Jul 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-1768-1645. Novel regulatory mechanisms of nuclear factor (NF)-𝛋B signaling: Novel regulatory mechanisms of nuclear factor (NF)-[kappa] B signaling. [Internet] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2152/47203.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-1768-1645. Novel regulatory mechanisms of nuclear factor (NF)-𝛋B signaling: Novel regulatory mechanisms of nuclear factor (NF)-[kappa] B signaling. [Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/47203

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

10. Ito, Yoshihiro. CP27: Expression, Regulation, and Function of a Chromatin Complex Member.

Degree: 2012, University of Illinois – Chicago

 CP27 is a novel gene involved in early vertebrate development that features a distinct expression pattern during development. The cp27 gene contains an open reading… (more)

Subjects/Keywords: CP27; NF-Y; USF1; chromatin complex; histone variant H2A.Z; Nanog; embryonic development; Craniofacial protein; Nuclear transcription factor Y; Nuclear transcription factor Y

…cooperative CCAAT boxes and identified the NF-Y transcription factor as the CCAAT activator… …that is regulated by the universal transcription factor NF-Y in combination with the USF-1… …conjunction with the NF-Y transcription factor as a crucial promoter organizer, facilitating the… …box binding factors is the ubiquitous transcription factor NF-Y, a trimeric transcriptional… …Nuclear transcription factor 1 Nuclear transcription factor Y Nuclear factor Y; Nuclear… 

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APA (6th Edition):

Ito, Y. (2012). CP27: Expression, Regulation, and Function of a Chromatin Complex Member. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9478

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ito, Yoshihiro. “CP27: Expression, Regulation, and Function of a Chromatin Complex Member.” 2012. Thesis, University of Illinois – Chicago. Accessed July 17, 2019. http://hdl.handle.net/10027/9478.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ito, Yoshihiro. “CP27: Expression, Regulation, and Function of a Chromatin Complex Member.” 2012. Web. 17 Jul 2019.

Vancouver:

Ito Y. CP27: Expression, Regulation, and Function of a Chromatin Complex Member. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10027/9478.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ito Y. CP27: Expression, Regulation, and Function of a Chromatin Complex Member. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9478

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

11. Μοσχονάς, Αριστείδης. Μελέτη μηχανισμών μεταγραφικής ρύθμισης από τον υποδοχέα CD40.

Degree: 2014, University of Crete (UOC); Πανεπιστήμιο Κρήτης

 We have previously shown that activation of CD40 induces IRF1 (1), a member of the IRF transcription family which acts as a master regulator of… (more)

Subjects/Keywords: Υποδοχέας CD40; Μονοπάτι NF-κΒ; Ιντερφερόνη - β; Μεταγραφικός παράγοντας IRF1; Μεταγραφικός παράγοντας IRF7; Κινάση TPL2; Κινάση ERK; CD40 receptor; NF- κΒ pathway; IFN - β; IRF1 transcription factor; IRF7 transcription factor; TPL2 kinase; ERK kinase

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APA (6th Edition):

Μοσχονάς, . . (2014). Μελέτη μηχανισμών μεταγραφικής ρύθμισης από τον υποδοχέα CD40. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/38406

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Μοσχονάς, Αριστείδης. “Μελέτη μηχανισμών μεταγραφικής ρύθμισης από τον υποδοχέα CD40.” 2014. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed July 17, 2019. http://hdl.handle.net/10442/hedi/38406.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Μοσχονάς, Αριστείδης. “Μελέτη μηχανισμών μεταγραφικής ρύθμισης από τον υποδοχέα CD40.” 2014. Web. 17 Jul 2019.

Vancouver:

Μοσχονάς . Μελέτη μηχανισμών μεταγραφικής ρύθμισης από τον υποδοχέα CD40. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10442/hedi/38406.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Μοσχονάς . Μελέτη μηχανισμών μεταγραφικής ρύθμισης από τον υποδοχέα CD40. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2014. Available from: http://hdl.handle.net/10442/hedi/38406

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

12. Farrow, Michael John. The effect of androstenediol on gene expression and NF-¿B activation in vitro.

Degree: PhD, Oral Biology, 2007, The Ohio State University

Transcription factor activation is a rapidly induced intermediary component of the innate immune response to lipopolysaccharide (LPS). Intracellular signaling cascades initiated by extracellular recognition of… (more)

Subjects/Keywords: Androstenediol; Glucocorticoid; Inflammation; Nuclear Factor Kappa B; NF-kappaB; p65; Chromatin Immunoprecipitation; TransAM; Transcription; Gene Expression; tumor necrosis factor alpha; TNF-alpha; cytokine

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APA (6th Edition):

Farrow, M. J. (2007). The effect of androstenediol on gene expression and NF-¿B activation in vitro. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1187109346

Chicago Manual of Style (16th Edition):

Farrow, Michael John. “The effect of androstenediol on gene expression and NF-¿B activation in vitro.” 2007. Doctoral Dissertation, The Ohio State University. Accessed July 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1187109346.

MLA Handbook (7th Edition):

Farrow, Michael John. “The effect of androstenediol on gene expression and NF-¿B activation in vitro.” 2007. Web. 17 Jul 2019.

Vancouver:

Farrow MJ. The effect of androstenediol on gene expression and NF-¿B activation in vitro. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Jul 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1187109346.

Council of Science Editors:

Farrow MJ. The effect of androstenediol on gene expression and NF-¿B activation in vitro. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1187109346


Oregon State University

13. Kyrylkova, Kateryna. The role of the transcriptional regulatory protein BCL11B in dental and craniofacial development.

Degree: PhD, Pharmacy, 2014, Oregon State University

 BCL11B is a transcriptional regulatory protein that plays essential roles during mouse embryonic development. BCL11B is expressed and functions in the immune and nervous systems… (more)

Subjects/Keywords: Transcription factor; Transcription factors

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APA (6th Edition):

Kyrylkova, K. (2014). The role of the transcriptional regulatory protein BCL11B in dental and craniofacial development. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/45238

Chicago Manual of Style (16th Edition):

Kyrylkova, Kateryna. “The role of the transcriptional regulatory protein BCL11B in dental and craniofacial development.” 2014. Doctoral Dissertation, Oregon State University. Accessed July 17, 2019. http://hdl.handle.net/1957/45238.

MLA Handbook (7th Edition):

Kyrylkova, Kateryna. “The role of the transcriptional regulatory protein BCL11B in dental and craniofacial development.” 2014. Web. 17 Jul 2019.

Vancouver:

Kyrylkova K. The role of the transcriptional regulatory protein BCL11B in dental and craniofacial development. [Internet] [Doctoral dissertation]. Oregon State University; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1957/45238.

Council of Science Editors:

Kyrylkova K. The role of the transcriptional regulatory protein BCL11B in dental and craniofacial development. [Doctoral Dissertation]. Oregon State University; 2014. Available from: http://hdl.handle.net/1957/45238

14. M. Lorenzo. THE INTERPLAY AMONG NF-Y AND E-BOX TRANSCRIPTION FACTORS: MAX, MYC AND USF1.

Degree: 2015, Università degli Studi di Milano

Transcription is a process finely regulated by different transcription factors (TFs) which bind regulatory sequences present in gene promoters and allow the precise execution of… (more)

Subjects/Keywords: Transcription Factors; NF-Y; E-BOX; interplay; Settore BIO/10 - Biochimica; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

Lorenzo, M. (2015). THE INTERPLAY AMONG NF-Y AND E-BOX TRANSCRIPTION FACTORS: MAX, MYC AND USF1. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/274117

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lorenzo, M.. “THE INTERPLAY AMONG NF-Y AND E-BOX TRANSCRIPTION FACTORS: MAX, MYC AND USF1.” 2015. Thesis, Università degli Studi di Milano. Accessed July 17, 2019. http://hdl.handle.net/2434/274117.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lorenzo, M.. “THE INTERPLAY AMONG NF-Y AND E-BOX TRANSCRIPTION FACTORS: MAX, MYC AND USF1.” 2015. Web. 17 Jul 2019.

Vancouver:

Lorenzo M. THE INTERPLAY AMONG NF-Y AND E-BOX TRANSCRIPTION FACTORS: MAX, MYC AND USF1. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2434/274117.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lorenzo M. THE INTERPLAY AMONG NF-Y AND E-BOX TRANSCRIPTION FACTORS: MAX, MYC AND USF1. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/274117

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

15. Atkinson, George P. (George Prescott). The peptidyl-prolyl isomerase Pin1 promotes NF-[kappa]B and STAT3 signaling in glioblastoma.

Degree: PhD, 2009, University of Alabama – Birmingham

Glioblastoma (GBM) is an incurable tumor of the central nervous system (CNS). Over the past 50 years, little progress has made in improving the quality… (more)

Subjects/Keywords: Glioblastoma  – pathology<; br>; Neoplasms<; br>; NF-kappa B  – metabolism<; br>; Peptidylprolyl Isomerase<; br>; STAT3 Transcription Factor

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APA (6th Edition):

Atkinson, G. P. (. P. (2009). The peptidyl-prolyl isomerase Pin1 promotes NF-[kappa]B and STAT3 signaling in glioblastoma. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,812

Chicago Manual of Style (16th Edition):

Atkinson, George P (George Prescott). “The peptidyl-prolyl isomerase Pin1 promotes NF-[kappa]B and STAT3 signaling in glioblastoma.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 17, 2019. http://contentdm.mhsl.uab.edu/u?/etd,812.

MLA Handbook (7th Edition):

Atkinson, George P (George Prescott). “The peptidyl-prolyl isomerase Pin1 promotes NF-[kappa]B and STAT3 signaling in glioblastoma.” 2009. Web. 17 Jul 2019.

Vancouver:

Atkinson GP(P. The peptidyl-prolyl isomerase Pin1 promotes NF-[kappa]B and STAT3 signaling in glioblastoma. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Jul 17]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,812.

Council of Science Editors:

Atkinson GP(P. The peptidyl-prolyl isomerase Pin1 promotes NF-[kappa]B and STAT3 signaling in glioblastoma. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,812


Universitat de Valencia

16. Bosch Campos, Ana. Role of the NF-kB pathway and nitric oxide in mammary gland involution after weaning. Implications in breast cancer .

Degree: 2013, Universitat de Valencia

 INTRODUCCIÓN La glándula mamaria es un órgano dinámico que alcanza su máximo desarrollo funcional con la lactancia, momento en el cual, a través de la… (more)

Subjects/Keywords: breast cancer; inflammation; apoptosis; cathepsin D; mammary gland involution; nitric oxide; NOS2-KO; nitrotyrosine; nuclear factor κappa B (NF-κB); weaning; signal transducer and activator of transcription (STAT)

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APA (6th Edition):

Bosch Campos, A. (2013). Role of the NF-kB pathway and nitric oxide in mammary gland involution after weaning. Implications in breast cancer . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/25626

Chicago Manual of Style (16th Edition):

Bosch Campos, Ana. “Role of the NF-kB pathway and nitric oxide in mammary gland involution after weaning. Implications in breast cancer .” 2013. Doctoral Dissertation, Universitat de Valencia. Accessed July 17, 2019. http://hdl.handle.net/10550/25626.

MLA Handbook (7th Edition):

Bosch Campos, Ana. “Role of the NF-kB pathway and nitric oxide in mammary gland involution after weaning. Implications in breast cancer .” 2013. Web. 17 Jul 2019.

Vancouver:

Bosch Campos A. Role of the NF-kB pathway and nitric oxide in mammary gland involution after weaning. Implications in breast cancer . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10550/25626.

Council of Science Editors:

Bosch Campos A. Role of the NF-kB pathway and nitric oxide in mammary gland involution after weaning. Implications in breast cancer . [Doctoral Dissertation]. Universitat de Valencia; 2013. Available from: http://hdl.handle.net/10550/25626


University of Missouri – Columbia

17. Dhar, Srijita. Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions.

Degree: 2009, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] ADAM 12 overexpression is linked to the pathology of diseases including osteoarthritis, cancer, cardiac hypertrophy,… (more)

Subjects/Keywords: Membrane proteins  – Physiological transport; Osteoarthritis  – Pathogenesis; Articular cartilage  – Metabolism; NF-kappa B (DNA-binding protein)  – Metabolism; Transforming growth factors-beta  – Metabolism; Bone cells  – Metabolism; Synovial membranes  – Metabolism; Metalloproteinases  – Metabolism; ADAM Proteins  – metabolism; Cartilage, Articular  – metabolism; Osteoarthritis  – pathology; Transforming Growth Factor beta  – pharmacology; NF-kappa B  – metabolism; Sp1 Transcription Factor  – metabolism; Osteoblasts  – metabolism; Synovial Membrane  – metabolism

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APA (6th Edition):

Dhar, S. (2009). Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/10290

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Dhar, Srijita. “Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions.” 2009. Thesis, University of Missouri – Columbia. Accessed July 17, 2019. https://doi.org/10.32469/10355/10290.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Dhar, Srijita. “Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions.” 2009. Web. 17 Jul 2019.

Vancouver:

Dhar S. Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions. [Internet] [Thesis]. University of Missouri – Columbia; 2009. [cited 2019 Jul 17]. Available from: https://doi.org/10.32469/10355/10290.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Dhar S. Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions. [Thesis]. University of Missouri – Columbia; 2009. Available from: https://doi.org/10.32469/10355/10290

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Case Western Reserve University

18. Dermawan, Josephine Kam Tai. From NF-¿B to FACT: Mechanisms and Translational Applications of EGFR-mediated NF-¿B Regulation.

Degree: PhD, Molecular Medicine, 2015, Case Western Reserve University

 The epidermal growth factor receptor (EGFR) drives downstream signaling pathways that promote cancer progression. EGFR is often constitutively active in tumors, e.g., non-small cell lung… (more)

Subjects/Keywords: Cellular Biology; Molecular Biology; Oncology; Genetics; ChIP-seq; CRISPR; epidermal growth factor receptor, EGFR; curaxins; facilitates chromatin transcription, FACT; glioblastoma; GBM stem cell; nuclear factor kappa B, NF-kappaB; non-small cell lung cancer; quinacrine; RNA-seq; transcriptional regulation

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APA (6th Edition):

Dermawan, J. K. T. (2015). From NF-¿B to FACT: Mechanisms and Translational Applications of EGFR-mediated NF-¿B Regulation. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1436292263

Chicago Manual of Style (16th Edition):

Dermawan, Josephine Kam Tai. “From NF-¿B to FACT: Mechanisms and Translational Applications of EGFR-mediated NF-¿B Regulation.” 2015. Doctoral Dissertation, Case Western Reserve University. Accessed July 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1436292263.

MLA Handbook (7th Edition):

Dermawan, Josephine Kam Tai. “From NF-¿B to FACT: Mechanisms and Translational Applications of EGFR-mediated NF-¿B Regulation.” 2015. Web. 17 Jul 2019.

Vancouver:

Dermawan JKT. From NF-¿B to FACT: Mechanisms and Translational Applications of EGFR-mediated NF-¿B Regulation. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2015. [cited 2019 Jul 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1436292263.

Council of Science Editors:

Dermawan JKT. From NF-¿B to FACT: Mechanisms and Translational Applications of EGFR-mediated NF-¿B Regulation. [Doctoral Dissertation]. Case Western Reserve University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1436292263


Queens University

19. Ferrant, Harriet Ann. Homo and hetero-dimerization studies of two Zn(II)2Cys6 transcription factors in fission yeast .

Degree: Biology, 2012, Queens University

 This thesis presents a strategy designed to determine how Thi1 and Thi5 may differentially regulate thiamine production and the vegetative and sexual life cycles in… (more)

Subjects/Keywords: Thi1; Thi5; Transcription factor; Thiamine

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APA (6th Edition):

Ferrant, H. A. (2012). Homo and hetero-dimerization studies of two Zn(II)2Cys6 transcription factors in fission yeast . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/7313

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ferrant, Harriet Ann. “Homo and hetero-dimerization studies of two Zn(II)2Cys6 transcription factors in fission yeast .” 2012. Thesis, Queens University. Accessed July 17, 2019. http://hdl.handle.net/1974/7313.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ferrant, Harriet Ann. “Homo and hetero-dimerization studies of two Zn(II)2Cys6 transcription factors in fission yeast .” 2012. Web. 17 Jul 2019.

Vancouver:

Ferrant HA. Homo and hetero-dimerization studies of two Zn(II)2Cys6 transcription factors in fission yeast . [Internet] [Thesis]. Queens University; 2012. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1974/7313.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ferrant HA. Homo and hetero-dimerization studies of two Zn(II)2Cys6 transcription factors in fission yeast . [Thesis]. Queens University; 2012. Available from: http://hdl.handle.net/1974/7313

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Penn State University

20. Tajiri, Momoko. Roles of Archaeal general transcription factors TFB1 and TFB2 in Thermococus Kodakarensis during heat stress response.

Degree: PhD, Integrative Biosciences, 2008, Penn State University

 This dissertation summarizes two projects concerning roles for homologues of a general transcription factor (GTF), called transcription factor B (TFB) during transcription regulation in Archaea.… (more)

Subjects/Keywords: general transcription factor; archaea; TFB

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APA (6th Edition):

Tajiri, M. (2008). Roles of Archaeal general transcription factors TFB1 and TFB2 in Thermococus Kodakarensis during heat stress response. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8925

Chicago Manual of Style (16th Edition):

Tajiri, Momoko. “Roles of Archaeal general transcription factors TFB1 and TFB2 in Thermococus Kodakarensis during heat stress response.” 2008. Doctoral Dissertation, Penn State University. Accessed July 17, 2019. https://etda.libraries.psu.edu/catalog/8925.

MLA Handbook (7th Edition):

Tajiri, Momoko. “Roles of Archaeal general transcription factors TFB1 and TFB2 in Thermococus Kodakarensis during heat stress response.” 2008. Web. 17 Jul 2019.

Vancouver:

Tajiri M. Roles of Archaeal general transcription factors TFB1 and TFB2 in Thermococus Kodakarensis during heat stress response. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2019 Jul 17]. Available from: https://etda.libraries.psu.edu/catalog/8925.

Council of Science Editors:

Tajiri M. Roles of Archaeal general transcription factors TFB1 and TFB2 in Thermococus Kodakarensis during heat stress response. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8925


University of Southern California

21. Skylar, Anna Maria. Genetic control of meristematic proliferation in Arabidopsis thaliana.

Degree: PhD, Molecular Biology, 2014, University of Southern California

 When a dormant seed of flowering plants receives environmental cues to begin germination, a remarkable series of transformation takes place. The seed coat cracks open,… (more)

Subjects/Keywords: meristems; Arabidopsis; transcription factor binding

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APA (6th Edition):

Skylar, A. M. (2014). Genetic control of meristematic proliferation in Arabidopsis thaliana. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458438/rec/2996

Chicago Manual of Style (16th Edition):

Skylar, Anna Maria. “Genetic control of meristematic proliferation in Arabidopsis thaliana.” 2014. Doctoral Dissertation, University of Southern California. Accessed July 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458438/rec/2996.

MLA Handbook (7th Edition):

Skylar, Anna Maria. “Genetic control of meristematic proliferation in Arabidopsis thaliana.” 2014. Web. 17 Jul 2019.

Vancouver:

Skylar AM. Genetic control of meristematic proliferation in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Jul 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458438/rec/2996.

Council of Science Editors:

Skylar AM. Genetic control of meristematic proliferation in Arabidopsis thaliana. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458438/rec/2996


University of Manchester

22. Webber, Aaron. Transcriptional co-regulation of microRNAs and protein-coding genes.

Degree: 2013, University of Manchester

 This thesis was presented by Aaron Webber on the 4th December 2013 for the degree of Doctor of Philosophy from the University of Manchester. The… (more)

Subjects/Keywords: MicroRNA; Transcription factor; Regulatory network

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APA (6th Edition):

Webber, A. (2013). Transcriptional co-regulation of microRNAs and protein-coding genes. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:214196

Chicago Manual of Style (16th Edition):

Webber, Aaron. “Transcriptional co-regulation of microRNAs and protein-coding genes.” 2013. Doctoral Dissertation, University of Manchester. Accessed July 17, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:214196.

MLA Handbook (7th Edition):

Webber, Aaron. “Transcriptional co-regulation of microRNAs and protein-coding genes.” 2013. Web. 17 Jul 2019.

Vancouver:

Webber A. Transcriptional co-regulation of microRNAs and protein-coding genes. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Jul 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:214196.

Council of Science Editors:

Webber A. Transcriptional co-regulation of microRNAs and protein-coding genes. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:214196

23. Tamura, Taizo. High-resolution analysis of DNA binding property of VND7, the master transcription factor for vessel cell differentiation : 道管分化マスター転写因子VND7のDNA結合特性に関する高解像度解析; ドウカン ブンカ マスター テンシャ インシ VND7 ノ DNA ケツゴウ トクセイ ニ カンスル コウカイゾウド カイセキ.

Degree: 博士(バイオサイエンス), 2017, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: Transcription factor

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APA (6th Edition):

Tamura, T. (2017). High-resolution analysis of DNA binding property of VND7, the master transcription factor for vessel cell differentiation : 道管分化マスター転写因子VND7のDNA結合特性に関する高解像度解析; ドウカン ブンカ マスター テンシャ インシ VND7 ノ DNA ケツゴウ トクセイ ニ カンスル コウカイゾウド カイセキ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/11517

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tamura, Taizo. “High-resolution analysis of DNA binding property of VND7, the master transcription factor for vessel cell differentiation : 道管分化マスター転写因子VND7のDNA結合特性に関する高解像度解析; ドウカン ブンカ マスター テンシャ インシ VND7 ノ DNA ケツゴウ トクセイ ニ カンスル コウカイゾウド カイセキ.” 2017. Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed July 17, 2019. http://hdl.handle.net/10061/11517.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tamura, Taizo. “High-resolution analysis of DNA binding property of VND7, the master transcription factor for vessel cell differentiation : 道管分化マスター転写因子VND7のDNA結合特性に関する高解像度解析; ドウカン ブンカ マスター テンシャ インシ VND7 ノ DNA ケツゴウ トクセイ ニ カンスル コウカイゾウド カイセキ.” 2017. Web. 17 Jul 2019.

Vancouver:

Tamura T. High-resolution analysis of DNA binding property of VND7, the master transcription factor for vessel cell differentiation : 道管分化マスター転写因子VND7のDNA結合特性に関する高解像度解析; ドウカン ブンカ マスター テンシャ インシ VND7 ノ DNA ケツゴウ トクセイ ニ カンスル コウカイゾウド カイセキ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2017. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10061/11517.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tamura T. High-resolution analysis of DNA binding property of VND7, the master transcription factor for vessel cell differentiation : 道管分化マスター転写因子VND7のDNA結合特性に関する高解像度解析; ドウカン ブンカ マスター テンシャ インシ VND7 ノ DNA ケツゴウ トクセイ ニ カンスル コウカイゾウド カイセキ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2017. Available from: http://hdl.handle.net/10061/11517

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

24. Schneider, Andrew. Investigating the Role of the VAL1 Transcription Factor in Arabidopsis thaliana Embryo Development.

Degree: PhD, Plant Pathology, Physiology, and Weed Science, 2015, Virginia Tech

 Developing oilseeds accumulate oils and seed storage proteins synthesized by the pathways of primary metabolism. Seed development and metabolism are positively regulated at the transcriptional… (more)

Subjects/Keywords: Arabidopsis; seeds; transcription factor; epigenetic

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APA (6th Edition):

Schneider, A. (2015). Investigating the Role of the VAL1 Transcription Factor in Arabidopsis thaliana Embryo Development. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/56694

Chicago Manual of Style (16th Edition):

Schneider, Andrew. “Investigating the Role of the VAL1 Transcription Factor in Arabidopsis thaliana Embryo Development.” 2015. Doctoral Dissertation, Virginia Tech. Accessed July 17, 2019. http://hdl.handle.net/10919/56694.

MLA Handbook (7th Edition):

Schneider, Andrew. “Investigating the Role of the VAL1 Transcription Factor in Arabidopsis thaliana Embryo Development.” 2015. Web. 17 Jul 2019.

Vancouver:

Schneider A. Investigating the Role of the VAL1 Transcription Factor in Arabidopsis thaliana Embryo Development. [Internet] [Doctoral dissertation]. Virginia Tech; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10919/56694.

Council of Science Editors:

Schneider A. Investigating the Role of the VAL1 Transcription Factor in Arabidopsis thaliana Embryo Development. [Doctoral Dissertation]. Virginia Tech; 2015. Available from: http://hdl.handle.net/10919/56694


University of Ottawa

25. Sarvan, Sabina. Structural and Functional Characterization of Campylobacter Jejuni Ferric Uptake Regulator (CjFur) .

Degree: 2018, University of Ottawa

 Transition metals are crucial components of several metabolic pathways and are critical for DNA, RNA and protein synthesis. However, when found in excess, these metal… (more)

Subjects/Keywords: X-ray crystallography; Transcription factor

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APA (6th Edition):

Sarvan, S. (2018). Structural and Functional Characterization of Campylobacter Jejuni Ferric Uptake Regulator (CjFur) . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37202

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sarvan, Sabina. “Structural and Functional Characterization of Campylobacter Jejuni Ferric Uptake Regulator (CjFur) .” 2018. Thesis, University of Ottawa. Accessed July 17, 2019. http://hdl.handle.net/10393/37202.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sarvan, Sabina. “Structural and Functional Characterization of Campylobacter Jejuni Ferric Uptake Regulator (CjFur) .” 2018. Web. 17 Jul 2019.

Vancouver:

Sarvan S. Structural and Functional Characterization of Campylobacter Jejuni Ferric Uptake Regulator (CjFur) . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10393/37202.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sarvan S. Structural and Functional Characterization of Campylobacter Jejuni Ferric Uptake Regulator (CjFur) . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37202

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


North Carolina State University

26. Wang, Tianyuan. Identifying Transcription Factor Targets and Studying Human Complex Disease Genes.

Degree: PhD, Bioinformatics, 2009, North Carolina State University

Transcription factors (TFs) have been characterized as mediators of human complex disease processes. The target genes of TFs also may be associated with disease. Identification… (more)

Subjects/Keywords: binding site; prediction; transcription factor

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APA (6th Edition):

Wang, T. (2009). Identifying Transcription Factor Targets and Studying Human Complex Disease Genes. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/3628

Chicago Manual of Style (16th Edition):

Wang, Tianyuan. “Identifying Transcription Factor Targets and Studying Human Complex Disease Genes.” 2009. Doctoral Dissertation, North Carolina State University. Accessed July 17, 2019. http://www.lib.ncsu.edu/resolver/1840.16/3628.

MLA Handbook (7th Edition):

Wang, Tianyuan. “Identifying Transcription Factor Targets and Studying Human Complex Disease Genes.” 2009. Web. 17 Jul 2019.

Vancouver:

Wang T. Identifying Transcription Factor Targets and Studying Human Complex Disease Genes. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2019 Jul 17]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3628.

Council of Science Editors:

Wang T. Identifying Transcription Factor Targets and Studying Human Complex Disease Genes. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3628


North Carolina State University

27. Yin, Haifeng. Expression and developmental requirement for transcription factor Sp2.

Degree: PhD, Functional Genomics, 2009, North Carolina State University

 The Sp-family of DNA-binding proteins is comprised by nine members, and controls the expression of many mammalian genes. Most Sp-family members have been well studied… (more)

Subjects/Keywords: transcription factor Sp2; development

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APA (6th Edition):

Yin, H. (2009). Expression and developmental requirement for transcription factor Sp2. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4630

Chicago Manual of Style (16th Edition):

Yin, Haifeng. “Expression and developmental requirement for transcription factor Sp2.” 2009. Doctoral Dissertation, North Carolina State University. Accessed July 17, 2019. http://www.lib.ncsu.edu/resolver/1840.16/4630.

MLA Handbook (7th Edition):

Yin, Haifeng. “Expression and developmental requirement for transcription factor Sp2.” 2009. Web. 17 Jul 2019.

Vancouver:

Yin H. Expression and developmental requirement for transcription factor Sp2. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2019 Jul 17]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4630.

Council of Science Editors:

Yin H. Expression and developmental requirement for transcription factor Sp2. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4630


University of Rochester

28. Ding, Qian. The Role of BARHL2 in the Neurogenesis of Mouse Retina and Spinal Cord.

Degree: PhD, 2010, University of Rochester

 The evolutionary conserved BarH family of homeodomain transcription factors plays essential roles in cell fate specification, cell differentiation, migration and survival by either activation or… (more)

Subjects/Keywords: Transcription Factor; Subtype; Neuron

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APA (6th Edition):

Ding, Q. (2010). The Role of BARHL2 in the Neurogenesis of Mouse Retina and Spinal Cord. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/9737

Chicago Manual of Style (16th Edition):

Ding, Qian. “The Role of BARHL2 in the Neurogenesis of Mouse Retina and Spinal Cord.” 2010. Doctoral Dissertation, University of Rochester. Accessed July 17, 2019. http://hdl.handle.net/1802/9737.

MLA Handbook (7th Edition):

Ding, Qian. “The Role of BARHL2 in the Neurogenesis of Mouse Retina and Spinal Cord.” 2010. Web. 17 Jul 2019.

Vancouver:

Ding Q. The Role of BARHL2 in the Neurogenesis of Mouse Retina and Spinal Cord. [Internet] [Doctoral dissertation]. University of Rochester; 2010. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1802/9737.

Council of Science Editors:

Ding Q. The Role of BARHL2 in the Neurogenesis of Mouse Retina and Spinal Cord. [Doctoral Dissertation]. University of Rochester; 2010. Available from: http://hdl.handle.net/1802/9737


University of New South Wales

29. Chavalit, Tanit. WDR5 is a novel partner of KLF3 and this interaction is important for KLF3 genomic localisation.

Degree: Biotechnology & Biomolecular Sciences, 2018, University of New South Wales

 Krüppel-like Factor 3 (KLF3) is a member of the Krüppel-like factor family and is a potent transcriptional repressor. KLF3 is comprised of two domains: a… (more)

Subjects/Keywords: Transcription factor; KLF3; WDR5

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APA (6th Edition):

Chavalit, T. (2018). WDR5 is a novel partner of KLF3 and this interaction is important for KLF3 genomic localisation. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60070

Chicago Manual of Style (16th Edition):

Chavalit, Tanit. “WDR5 is a novel partner of KLF3 and this interaction is important for KLF3 genomic localisation.” 2018. Doctoral Dissertation, University of New South Wales. Accessed July 17, 2019. http://handle.unsw.edu.au/1959.4/60070.

MLA Handbook (7th Edition):

Chavalit, Tanit. “WDR5 is a novel partner of KLF3 and this interaction is important for KLF3 genomic localisation.” 2018. Web. 17 Jul 2019.

Vancouver:

Chavalit T. WDR5 is a novel partner of KLF3 and this interaction is important for KLF3 genomic localisation. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2019 Jul 17]. Available from: http://handle.unsw.edu.au/1959.4/60070.

Council of Science Editors:

Chavalit T. WDR5 is a novel partner of KLF3 and this interaction is important for KLF3 genomic localisation. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/60070

30. Sevdali, Eirini. Μελέτη του σηματοδοτικού μονοπατιού BAFF/APRIL στην οξεία λεμφοβλαστική λευχαιμία.

Degree: 2018, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας

BAFF and APRIL are master regulators of survival, maturation and homeostasis of normal developing B-cells, by interacting with three cognate receptors, BAFFR, TACI and BCMA.… (more)

Subjects/Keywords: Β-οξεία λεμφοβλαστική λευχαιμία; BAFF/APRIL σύστημα; Υποδοχέας BAFFR; Συνδέτης BAFF; Μεταγραφικός παράγοντας E2A-PBX1; Εναλλακτική οδός του NF-κB2; Γλυκοκορτικοειδή; Απόπτωση; Χρωμοσωμική μετατόπιση BCR-ABL; B-cell acute lymphoblastic leukemia; BAFF/APRIL system; BAFFR receptor; BAFF ligand; Transcription factor E2A-PBX1; Alternative pathway of NF-κB2; Glucocorticoids; Apoptosis; Chromosomal translocation BCR-ABL

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Sevdali, E. (2018). Μελέτη του σηματοδοτικού μονοπατιού BAFF/APRIL στην οξεία λεμφοβλαστική λευχαιμία. (Thesis). University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Retrieved from http://hdl.handle.net/10442/hedi/42864

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sevdali, Eirini. “Μελέτη του σηματοδοτικού μονοπατιού BAFF/APRIL στην οξεία λεμφοβλαστική λευχαιμία.” 2018. Thesis, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Accessed July 17, 2019. http://hdl.handle.net/10442/hedi/42864.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sevdali, Eirini. “Μελέτη του σηματοδοτικού μονοπατιού BAFF/APRIL στην οξεία λεμφοβλαστική λευχαιμία.” 2018. Web. 17 Jul 2019.

Vancouver:

Sevdali E. Μελέτη του σηματοδοτικού μονοπατιού BAFF/APRIL στην οξεία λεμφοβλαστική λευχαιμία. [Internet] [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2018. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10442/hedi/42864.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sevdali E. Μελέτη του σηματοδοτικού μονοπατιού BAFF/APRIL στην οξεία λεμφοβλαστική λευχαιμία. [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2018. Available from: http://hdl.handle.net/10442/hedi/42864

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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